Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL115020

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
C=CCN(C)CCCCCCOc1ccc(C(=O)c2ccc(Br)cc2)c(OC)c1.O=C(O)/C=C/C(=O)O

Basic Information

ChEMBL ID CHEMBL115020
Phase Preclinical
Structure Type MOL
InChI Key DXGFLMIDYUDUND-WLHGVMLRSA-N
Parent Compound CHEMBL611485
Active Moiety CHEMBL611485
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

460.4
MW (Da)
5.75
ALogP
4
HBA
0
HBD
38.8
PSA (Ų)
0.22
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H34BrNO7
MW 576.48
Aromatic Rings 2
Heavy Atoms 29
NP-Likeness -0.76

Activity Summary

IC50 1 meas. best 8.34

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Lanosterol synthase
CHEMBL3593
IC50 8.34 8.34 4.6 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Lanosterol synthase IC50 = 4.6 nM 8.34 In vitro inhibition of human 2,3-oxidosqualene cyclase. 12852766

Literature References

PubMed DOI Target Context # Activities
12852766 10.1021/jm021120f Lanosterol synthase 4

Data from ChEMBL 36 via Core Engine